450849003: Congenital monosaccharide malabsorption (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Congenital monosaccharide malabsorption
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Congenital monosaccharide malabsorption
\Digestive system finding (finding)\Disorder of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Congenital monosaccharide malabsorption

\Disease\Fetal and/or neonatal disorder\Congenital disease\Congenital monosaccharide malabsorption
\Disease\Fetal and/or neonatal disorder\Disorder of digestive system specific to fetus OR newborn\Congenital monosaccharide malabsorption
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of gastrointestinal tract (disorder)\Malabsorption syndrome\Congenital monosaccharide malabsorption
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Congenital monosaccharide malabsorption
\Disease\Metabolic disease\Disorder of carbohydrate metabolism\Disorder of carbohydrate absorption\Congenital monosaccharide malabsorption

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2012. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2920590011 Congenital monosaccharide malabsorption en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2920890015 Congenital monosaccharide malabsorption (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5884981000241119 malabsorption monosaccharidique congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5884991000241117 malabsorption congénitale d'un monosaccharide fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital monosaccharide malabsorption	Is a	Disorder of carbohydrate absorption	true	Inferred relationship	Some
Congenital monosaccharide malabsorption	Is a	Congenital disease	true	Inferred relationship	Some
Congenital monosaccharide malabsorption	Occurrence	Congenital	true	Inferred relationship	Some	1
Congenital monosaccharide malabsorption	Is a	Malabsorption syndrome	true	Inferred relationship	Some
Congenital monosaccharide malabsorption	Finding site	Oesophagus, stomach, small intestine and large intestine together as a single entity.	true	Inferred relationship	Some	2
Congenital monosaccharide malabsorption	Is a	Disorder of digestive system specific to fetus OR newborn	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
malabsorption congénitale du glucose-galactose	Is a	False	Congenital monosaccharide malabsorption	Inferred relationship	Some

This concept is not in any reference sets